Fe_3O_4/Py/PAM磁性荧光纳米粒子的制备及应用于废水中Cr(VI)的测定

本文采用层层自组装法合成了具有良好水溶性的功能化磁性荧光Fe3O4/Py(芘)/PAM(聚丙烯酰胺)纳米粒子.利用其磁性,能够对该粒子进行简单有效的分离纯化,并可以对待测粒子进行富集以提高其检测灵敏度.利用Cr(VI)对该复合粒子水溶液的荧光猝灭,建立了测定Cr(VI)的荧光分析法,讨论了反应机理.在最佳实验条件下,该方法的线性区间为0.1～14.0μgmL-1,检测限为0.02μgmL-1.常见的共存离子不干扰测定,该方法可用于环境废水中Cr(VI)的测定.     

Fe3O4/Py/PAM磁性荧光纳米粒子的制备及应用于废水中Cr(VI)的测定

本文采用层层自组装法合成了具有良好水溶性的功能化磁性荧光Fe₃O₄/Py(芘)/ PAM(聚丙烯酰胺)纳米粒子. 利用其磁性, 能够对该粒子进行简单有效的分离纯化, 并可以对待测粒子进行富集以提高其检测灵敏度. 利用Cr(VI)对该复合粒子水溶液的荧光猝灭, 建立了测定Cr(VI)的荧光分析法, 讨论了反应机理. 在最佳实验条件下, 该方法的线性区间为0.1~14.0 μg mL⁻¹, 检测限为0.02 μg mL⁻¹. 常见的共存离子不干扰测定, 该方法可用于环境废水中Cr(VI)的测定.     

Selective fluorescence determination of chromium (VI) in water samples with terbium composite nanoparticles

The strong fluorescence Tb/acetyl acetone (acac)/Poly (Acrylamide) (PAM) composite nanoparticles have been prepared under ultrasonic radiation. The nanoparticles were water-soluble, stable and have extremely narrow emission bands and high internal quantum efficiencies. Based on the fluorescence quenching of Tb/acac/PAM by Cr (VI), a method for the selective determination of Cr (VI), without separation of Cr (III) in water, was developed. The reaction condition between Cr (VI) and Tb/acac/PAM were investigated in detail. Under optimal experimental conditions, the linear calibration curve was obtained over the concentration range of 5-600 ng mL(-1) with a correlation coefficient of 0.9939. The corresponding detection limit is 0.8 ng mL(-1) and the relative standard deviation is 1.5% for 0.05 microg mL(-1) (n=7). The proposed method has been applied to the selective quantification of Cr (VI) in synthetic samples and waste-water samples with the satisfactory results. The assay is characterized by short reaction time, very few interference, stable fluorescence signals, simple instrument and simplicity.     

Preparation and application of a novel core/shell organic nanoparticle as a fluorescence probe in the selective determination of Cr(VI)

A novel core/shell organic nanoparticles, anthracene/poly-acrylamide (AN/PAM), has been prepared successfully. Based on the fluorescence quenching of AN/PAM nanoparticles by Cr(VI), a method for the selective determination of Cr(VI), without separation of Cr(VI) in water, was developed. Furthermore, the reaction mechanism between nano-AN/PAM and Cr(VI) was also discussed. The synthesis and reaction conditions were investigated in detail. The assay is characterized by short reaction time, very few interference stable fluorescence signals, simple instruments and sensitivity. Under optical experimental conditions, a limit of detection of 0.02 microg/ml was achieved. The calibration curve was linear over the concentration range 0.04-2.00 microg/ml with a correlation coefficient of 0.9924. The proposed method has been applied to the selective quantification of Cr(VI) in synthetic samples and waste-water samples with the satisfactory results.     

Synthesis and characterization of magnetic and luminescent Fe_3O_4/CdTe nanocomposites using aspartic acid as linker

In this study,the preparation of a new kind of magnetic and luminescent Fe₃O₄/CdTe nanocomposites was demonstrated. Superparamagnetic Fe₃O₄ nanoparticles were first synthesized by hydrothermal coprecipitation of ferric and ferrous ions,followed by the modification of their surfaces with tetramethylammonium hydroxide（TMAOH） and the chemical activation with aspartic acid.The surface-modified Fe₃O₄ nanoparticles were then covalently coated with CdTe quantum dots（QDs）,which were modified with mercaptoacetic acid（MPA）,to form the Fe₃O₄/CdTe magnetic and luminescent nanocomposites through the coordination of the amino groups on the surfaces of Fe₃O₄ and the carboxyl groups on CdTe QDs.The structure and properties of as-synthesized nanocomposites were characterized.It was indicated that the nanocomposites possessed structure with an average diameter of 40- 50 nm,yellow-green emission feature and room temperature ferro-magnetism.Both the fluorescence and UV-vis absorption spectra of the nanocomposites showed a blue shift comparing with those of CdTe QDs.The mechanism of the blue shift was presented.The nanocomposites retained the ferromagnetic property with a saturation magnetization of 8.9 emu/g.     

Novel magnetic and fluorescent nanocomposite as a sensitive probe for the determination of proteins

The Fe(3)O(4)/(sodium oleic acid/ethyltrimethyl ammonium bromide)(n)/4-aminobenzoic acid (Fe(3)O(4)/(NaOL/CTAB)(n)/PABA) nanocomposites have been prepared by a layer-by-layer self-assembly approach. This kind of nanocomposites have fluorescent, magnetic and water-soluble properties. Taking advantage of the magnetic property of nanocomposites, we can separated them from solution easily by using a permanent magnet. By using their strong fluorescence, we can detect proteins. At pH 6.98, the fluorescence of Fe(3)O(4)/(NaOL/CTAB)(n)/PABA nanocomposites can be enhanced by the proteins. Under optimal conditions, the linear ranges of calibration curves were 0.2-20, 0.2-13, 0.2-10 microg mL(-1) for gamma-globulin (gamma-IgG), human serum albumin (HSA), and bovine serum albumin (BSA), respectively. The detection limits were 0.02, 0.01, 0.02 for gamma-IgG, HSA and BSA, respectively. The method has been applied to analyze the total proteins in human samples and the results were in good agreement with those reported by the hospital. This method is sensitive, simple and potential in many areas.     

荧光磁性双功能树状分子微球的制备与表征

采用化学共沉淀法, 以FeCl₃·6H₂O和FeSO₄·7H₂O为原料制备了磁性Fe₃O₄纳米颗粒, 采用树状大分子对其进行修饰, 然后通过树状大分子具有的大量空腔及末端丰富的氨基, 经吸附、 键合, 与大量巯基乙酸修饰的CdSe/CdS量子点连接, 得到三代具有荧光磁性双功能的树状分子微球, 并对其进行结构表征与性能测试. 结果表明: 三代复合后的微球的平均粒径分别为15, 34和49 nm; 一代荧光磁性微球的发光性能最佳, 其量子产率达24.1%; 零代荧光磁性微球磁性能最优, 其饱和磁化强度为15.96 A·m²/kg. 这种具有荧光和磁性的双功能纳米复合微粒有望在免疫检测、 靶向治疗、 荧光追踪和磁性分离等方面得到广泛应用.     

Fe_3O_4/CdTe/聚氨酯纳米复合物的制备及其性能研究

由共沉淀法和Stober法制备了伯胺基功能化SiO2稳定的Fe3O4磁性纳米粒子Fe3O4@SiO2-NH2;Fe3O4@SiO2-NH2与二异氰酸酯及咪唑阳离子二醇、聚乙二醇的反应使其表面形成阳离子型聚氨酯稳定层;通过阳离子型聚氨酯与CdTe量子点表面修饰的巯基乙酸间的电荷相互作用,制备得到了Fe3O4/CdTe/聚氨酯纳米复合物.用X射线衍射(XRD)、红外吸收光谱(FTIR)、热重分析(TGA)、透射电子显微镜(TEM)、磁强计(VSM)、紫外吸收光谱(UV)、荧光发射光谱(PL)表征了该纳米复合物的结构与性能.结果表明,CdTe量子点均匀地分散在Fe3O4@SiO2磁性纳米粒子周围,所得纳米复合物在溶剂中分散均匀,不团聚,且具有超顺磁性,并保持了CdTe量子点的荧光性能.     

Preparation of surface plasmon resonance biosensor based on magnetic core/shell Fe3O4/SiO2 and Fe3O4/Ag/SiO2 nanoparticles

In this paper, surface plasmon resonance biosensors based on magnetic core/shell Fe(3)O(4)/SiO(2) and Fe(3)O(4)/Ag/SiO(2) nanoparticles were developed for immunoassay. With Fe(3)O(4) and Fe(3)O(4)/Ag nanoparticles being used as seeding materials, Fe(3)O(4)/SiO(2) and Fe(3)O(4)/Ag/SiO(2) nanoparticles were formed by hydrolysis of tetraethyl orthosilicate. The aldehyde group functionalized magnetic nanoparticles provide organic functionality for bioconjugation. The products were characterized by scanning electronic microscopy (SEM), transmission electronic microscopy (TEM), FTIR and UV-vis absorption spectrometry. The magnetic nanoparticles possess the unique superparamagnetism property, exceptional optical properties and good compatibilities, and could be used as immobilization matrix for goat anti-rabbit IgG. The magnetic nanoparticles can be easily immobilized on the surface of SPR biosensor chip by a magnetic pillar. The effects of Fe(3)O(4)/SiO(2) and Fe(3)O(4)/Ag/SiO(2) nanoparticles on the sensitivity of SPR biosensors were also investigated. As a result, the SPR biosensors based on Fe(3)O(4)/SiO(2) nanoparticles and Fe(3)O(4)/Ag/SiO(2) nanoparticles exhibit a response for rabbit IgG in the concentration range of 1.25-20.00 μg ml(-1) and 0.30-20.00 μg ml(-1), respectively.     

Photoluminescent Fe3O4/carbon nanocomposite with magnetic property

Fe(3)O(4)/carbon nanocomposite has been prepared by a facile chemical method, and characterized by X-ray diffraction, X-ray photoelectron spectroscopy, transmission electron microscopy, fourier transform infrared spectroscopy and scanning electron microscopy. The fluorescent and magnetic properties of the sample were investigated by fluorescence spectroscopy and vibrating-sample magnetometer, respectively. The results indicate that the Fe(3)O(4)/carbon nanocomposite exhibit good photoluminescent (emission ranging from 425 to 550 nm) and strong magnetic (saturation magnetization of 44.2 emu/g) properties.     

Preparation and characterization of thermosensitive polymers grafted onto silica-coated iron oxide nanoparticles

In this study, multifunctional nanoparticles containing thermosensitive polymers grafted onto the surfaces of 6-nm monodisperse Fe(3)O(4) magnetic nanoparticles coated by silica were synthesized using reverse microemulsions and free radical polymerization. The magnetic properties of SiO(2)/Fe(3)O(4) nanoparticles show superparamagnetic behavior. Thermosensitive PNIPAM (poly(N-isopropylacrylamide)) was then grafted onto the surfaces of SiO(2)/Fe(3)O(4) nanoparticles, generating thermosensitive and magnetic properties of nanocomposites. The sizes of fabricated nanoparticles with core-shell structure are controlled at about 30 nm and each nanoparticle contains only one monodisperse Fe(3)O(4) core. For thermosensitivity analysis, the phase transition temperatures of multifunctional nanoparticles measured using DSC was at around 34-36 degrees C. The magnetic characteristics of these multifunctional nanoparticles were also superparamagnetic.     

Magnetic hard/soft nanocomposite ferrite aligned hollow microfibers and remanence enhancement

The nanocomposite SrFe(12)O(19)/Ni(0.5)Zn(0.5)Fe(2)O(4) ferrite aligned hollow microfibers with the hollow diameter to the fiber diameter estimated about 3/5 have been prepared by the gel precursor transformation process. The nanocomposite binary ferrites with different mass ratios are formed after the precursor calcined at 900°C for 2h, fabricating from SrFe(12)O(19) nanoparticles and Ni(0.5)Zn(0.5)Fe(2)O(4) nanoparticles with a uniform phase distribution. These nanocomposite ferrite microfibers show a combination of magnetic characteristics for the hard (SrFe(12)O(19)) and soft (Ni(0.5)Zn(0.5)Fe(2)O(4)) phase with an enhanced remanence owing to the exchange-coupling interactions. The aligned microfibers exhibit a shape anisotropy.     

Preparation of fluorescent polyvinyl alcohol keto-derivatives nanoparticles and selective determination of chromium(VI)

A novel fluorescent polyvinyl alcohol keto-derivatives nanoparticle (PVAK) has been prepared in one-step method. The nanoparticles has excitation and emission maxima at 349 and 462 nm, respectively. Based on the fluorescence quenching of PVAK by Cr(VI), we established a simple and selective fluorimetric method for the determination of Cr(VI) without separation of Cr(III) in water. The reaction conditions between Cr(VI) and PVAK were investigated in detail. Furthermore, the reaction mechanism between PVAK and Cr(VI) was also discussed. Under optimal experimental conditions, a limit of detection of 0.02 microg mL(-1) was achieved. The calibration curve was linear over the concentration range 0.1-13.2 microg mL(-1) with a correlation coefficient of 0.9987. The proposed method has been applied to the selective quantification of Cr(VI) in synthetic samples and waste-water samples with the satisfactory results.     

聚(苯胺-吡咯)共聚物/Fe3O4网状纳米纤维复合物的制备及吸波性能

在十六烷基三甲基溴化胺（CTAB）存在下,将苯胺（An）与吡咯（Py）两种单体在Fe3O4磁流体中原位化学氧化共聚制备了PAn-co-PPy/Fe3O4网状纳米纤维复合材料。通过改变CTAB的浓度、An/Py单体的配比及Fe3O4磁流体的用量获得了形态和电磁性能可调控的纳米纤维复合物。采用SEM、TEM、XRD、TG、电导和磁性能测试对复合物进行了表征,通过矢量网络分析仪获得了试样在2-18 GHz范围的复介电常数和复磁导率,经计算获取相应的微波反射损耗曲线。结果表明共聚复合物具有比单一的聚合物、共聚物、PAn/Fe3O4及PPy/Fe3O4更优越的微波吸收性能,样品（含Fe3O412.4 wt%）在9.0 GHz处具有最大的反射损耗为 -36.5 dB,损耗超过 -10 dB的频带宽度达4.7 GHz。     

磁性Fe_3O_4@PS@PAMAM-Ag复合催化粒子的制备及其可再生催化性能(英文)

采用聚苯乙烯(PS)包裹Fe3O4磁性纳米粒子,制得Fe3O4@PS复合微球,以此作为磁性载体,通过微球表面的羧基将聚酰胺-胺类树形大分子(PAMAM)连接到磁性载体上,然后使Ag纳米粒子镶嵌在树形分子层中,制得可再生的金属复合催化粒子Fe3O4@PS@PAMAM-Ag.并采用红外光谱、扫描电镜、电感耦合等离子体质谱(ICP-MS)和X射线光电子能谱等方法对复合催化粒子进行了表征,结果表明,树形分子可以较好地分散和稳定金属Ag纳米粒子,所制复合催化粒子表面Ag含量为1.64%,具有较高的催化还原对硝基苯酚的活性.同时,利用外加磁场可以方便快捷地从反应体系中分离出来,继续用于下一次反应中,复合催化粒子循环使用6次后,仍保持完全的催化性能.     

Fe3O4/Polypyrrole/Au nanocomposites with core/shell/shell structure: synthesis, characterization, and their electrochemical properties

Uniform Fe3O4 nanospheres with a diameter of 100 nm were rapidly prepared using a microwave solvothermal method. Then Fe304/polypyrrole (PPy) composite nanospheres with well-defined core/shell structures were obtained through chemical oxidative polymerization of pyrrole in the presence of Fe3O4; the average thickness of the coating shell was about 25 nm. Furthermore, by means of electrostatic interactions, plentiful gold nanoparticles with a diameter of 15 nm were assembled on the surface of Fe3O4/PPy to get Fe3O4/PPy/Au core/shell/shell structure. The morphology, structure, and composition of the products were characterized by transmission electronic microscopy (TEM), scanning electronic microscopy (SEM), X-ray powder diffraction (XRD), and Fourier transform infrared (FT-IR) spectroscopy. The resultant nanocomposites not only have the magnetism of Fe3O4 nanoparticles that make the nanocomposites easily controlled by an external magnetic field but also have the good conductivity and excellent electrochemical and catalytic properties of PPy and Au nanoparticles. Furthermore, the nanocomposites showed excellent electrocatalytic activities to biospecies such as ascorbic acid (AA).     

表面引发原子转移自由基聚合方法合成Fe3O4/PMMA复合纳米微粒

采用表面引发原子转移自由基聚合方法合成了核壳结构的磁性高分子纳米微粒. 作为聚合反应引发剂的3-氯丙酸, 首先与油酸修饰的Fe3O4纳米微粒表面的部分油酸置换, 然后在Fe3O4纳米微粒表面引发甲基丙烯酸甲酯聚合, 合成的纳米复合材料用TEM, FTIR, XRD和DSC表征. 磁性测试结果表明, 所制备的磁性高分子纳米微粒仍具有超顺磁性, 但由于聚合物的存在, 其饱和磁化强度降低.     

Exchange‐Coupled fct‐FePd/α‐Fe Nanocomposite Magnets Converted from Pd/Fe3O4 Core/Shell Nanoparticles

We report the controlled synthesis of exchange‐coupled face‐centered tetragonal (fct) FePd/α‐Fe nanocomposite magnets with variable Fe concentration. The composite was converted from Pd/Fe₃O₄ core/shell nanoparticles through a high‐temperature annealing process in a reducing atmosphere. The shell thickness of core/shell Pd/Fe₃O₄ nanoparticles could be readily tuned, and subsequently the concentration of Fe in nanocomposite magnets was controlled. Upon annealing reduction, the hard magnetic fct‐FePd phase was formed by the interdiffusion between reduced α‐Fe and face‐centered cubic (fcc) Pd, whereas the excessive α‐Fe remained around the fct‐FePd grains, realizing exchange coupling between the soft magnetic α‐Fe and hard magnetic fct‐FePd phases. Magnetic measurements showed variation in the magnetic properties of the nanocomposite magnets with different compositions, indicating distinct exchange coupling at the interfaces. The coercivity of the exchange‐coupled nanocomposites could be tuned from 0.7 to 2.8 kOe and the saturation magnetization could be controlled from 93 to 160 emu g^?1. This work provides a bottom‐up approach using exchange‐coupled nanocomposites for engineering advanced permanent magnets with controllable magnetic properties.     

Synthesis and characterization of multifunctional Fe3O4/poly(fluorescein O-methacrylate) core/shell nanoparticles

Multifunctional fluorescent and superparamagnetic Fe(3)O(4)/poly(fluorescein O-methacrylate) [Fe(3)O(4)/poly(FMA)] nanoparticles with core/shell structure were synthesized via surface-initiated polymerization. First, polymerizable double bonds were introduced onto the surface of Fe(3)O(4) nanoparticles via ligand exchange and a condensation reaction. A fluorescent monomer, FMA, was then polymerized to the double bonds at the surface via free-radical polymerization, leading to form a fluorescent polymer shell around the superparamagnetic Fe(3)O(4) core. The resultant Fe(3)O(4)/poly(FMA) nanoparticles were characterized by Fourier transform infrared, nuclear magnetic resonance, and X-ray diffraction spectroscopy to confirm the reactions. Transmission electron microscopy images showed that the Fe(3)O(4)/poly(FMA) nanoparticles have a spherical and monodisperse core/shell morphology. Photoluminescence spectroscopy and superconducting quantum interference device magnetometer analyses confirmed that the Fe(3)O(4)/poly(FMA) nanoparticles exhibited fluorescent and superparamagnetic properties, respectively. In addition, we demonstrated the potential bioimaging application of the Fe(3)O(4)/poly(FMA) nanoparticles by visualizing the cellular uptake of the nanoparticles into A549 lung cancer cells.     

Polyacrylamide/reduced graphene oxide-Ag nanocomposite as highly efficient antibacterial transparent film

In this study, preparation and characterization of polyacrylamide/reduced graphene oxide-Ag (PAM/rGO-Ag) nanocomposites as a new nanocomposite film were investigated. First, PAM/GO nanocomposite was synthesized by in situ polymerization strategy. Afterward, highly stable and uniformly distributed silver nanoparticles (Ag NPs) have been obtained with PAM/GO nanocomposite as nanoreactors via in situ reduction of silver nitrate (AgNO₃) using sodium borohydride (NaBH₄) as reducing agent. In addition, the prepared PAM/rGO-Ag nanocomposite was thermally annealed in order to achieve high-performance nanocomposite film with antimicrobial activities. The prepared nanocomposite was characterized by XRD, FT-IR, SEM, TEM and TGA. The obtained results demonstrate that the silver nanoparticles were well decorated and dispersed on the graphene oxide nanosheets. In fact, the GO nanosheets and polyacrylamide chains act as a support and stabilize the Ag nanoparticles. Moreover, antimicrobial activities of the films were also examined, and the films containing well-dispersed and stabilized Ag nanoparticles showed outstanding antibacterial activity.